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Kreativ, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
5
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K990060
MACH 7
June 15, 2000
K983227
POWER BLOCK
December 11, 1998
K980216
KREATIV MACH 5, MACH 5 PLUS, MACH M, MACH 6
June 16, 1998
K962376
KREATIV KURING LIGHT SYSTEM
March 21, 1997
K940776
KREATIV MODEL KV-1
December 21, 1994